Canonical Allele Identifier: PA2826443375
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1462026
ClinVar RCV Id: RCV001968252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Asp245Glu
CA342820316
NM_001257374.3:c.735C>A
CA342820317
NM_001257374.3:c.735C>G